Diaphragm Pacing System

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We have already had the testing done at the Cleveland Hospital. He qualifies but no one mentioned to us anything about a study that covers the costs. May I ask why you decided it wasn't for you?
 
I don't know much about the details of the study, but I originally inquired soley about the study. I was told it did exist but that the doctor hand picked the participants and that he was very selective.

I have thought about my condition and how much suffering I wanted to accept and also put my family through. I decided that I do not want to extend the poor quality of life that it appears I would have if the progression of my bulbar ALS continues. If my ALS were slow moving in my hands or feet, I think this would be a more viable option.

I also think that the cost is high if you are only going to gain a short time. If insurance were picking up the cost, it appears to be a better way to go than a ventilator. One day I believe DPS will be covered and preferred by all over the vent. I can't believe that it hasn't gained more acceptance already.
 
Natural, I appreciate your candor, thank you. My husband's onset was his legs. He still gets around pretty good and we are able to do lots. We were hoping this system would keep him off a vent so he can enjoy as much as possible. They are so close to FDA approval but i'm not sure he will still qualify by then.
 
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